SCHILLER
Appareils d'ecg, de diagnostic cardiopulmonaire et de surveillance des patients.
SCHILLER fabrique des appareils d'ECG, de diagnostic cardio-pulmonaire et de surveillance des patients à partir de ses opérations de Baar. La société fournit des systèmes de santé, des laboratoires, des partenaires OEM ou des clients exportateurs réglementés sur ses principaux marchés cotés.
- Type
- brand seeking distribution
- Location
- Baar, Switzerland
- Founded
- 1974
- Website
- schiller.ch
- Categories
- Fournitures médicales et de santé
- Markets
- Suisse, États-Unis, Allemagne, Japon
Verified facts
- certificate-page-on-site (amber), checked 2026-08-11 Company's own certification page
- places-goods-on-market (green), checked 2026-08-21 Swissmedic, swissdamed register of Swiss and Liechtenstein economic operators for medical devices
- registered-manufacturer (green), checked 2026-08-21 Swissmedic, swissdamed register of Swiss and Liechtenstein economic operators for medical devices
- fda-registered (green), checked 2026-07-21 FDA
- sanctions-clear (green), checked 2026-07-21 OpenSanctions
- registry-active-global (green), checked 2026-07-21 Zefix (Swiss commercial registry)
- lei-lapsed (amber), checked 2026-07-21 GLEIF
Claimed certifications
- ISO 13485, Medical Devices Quality IAF CertSearch
- CE Marking EU NANDO (notified bodies)
- FDA Registered FDA Establishment Registration
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)